White Shark Carcharodon Carcharias
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The Siege of Fort Beauséjour by Chris M. Hand Notes
1 The Siege of Fort Beauséjour by Chris M. Hand Notes Early Conflict in Nova Scotia 1604-1749. By the end of the 1600’s the area was decidedly French. 1713 Treaty of Utrecht After nearly 25 years of continuous war, France ceded Acadia to Britain. French and English disagreed over what actually made up Acadia. The British claimed all of Acadia, the current province of New Brunswick and parts of the current state of Maine. The French conceded Nova Scotia proper but refused to concede what is now New Brunswick and northern Maine, as well as modern Prince Edward Island and Cape Breton. They also chose to limit British ownership along the Chignecto Isthmus and also harboured ambitions to win back the peninsula and most of the Acadian settlers who, after 1713, became subjects of the British Crown. The defacto frontier lay along the Chignecto Isthmus which separates the Bay of Fundy from the Northumberland Strait on the north. Without the Isthmus and the river system to the west, France’s greatest colony along the St. Lawrence River would be completely cut off from November to April. Chignecto was the halfway house between Quebec and Louisbourg. 1721 Paul Mascarene, British governor of Nova Scotia, suggested that a small fort could be built on the neck with a garrison of 150 men. a) one atthe ridge of land at the Acadian town of Beaubassin (now Fort Lawrence) or b) one more west on the more prominent Beauséjour ridge. This never happened because British were busy fighting Mi’kmaq who were incited and abetted by the French. -
The Quest for Lobster Stock Boundaries in the Canadian
NOT TO BE CITED WITHOUT PRIOR REFERENCE TO THE AUTHOR(S) Northwest Atlantic Fisheries Organization Serial No. N615 NAFO SCR Doc. 82/IX/107 FOURTH ANNUAL MEETING - SEPTEMBER 1982 The Quest for Lobster Stoclg Boundaries in the Canadian Maritimes by A. Camp ell and R. K. Mohnl Invertebrates and Marine Plants Division Fisheries Research Branch, Department of Fisheries and Oceans Biological Station, St. Andrews, N. B., Canada EOG 2X0 P. O. Box 550, H lifax, N. S., Canada B3J 2S7 Abstract Historical and recent datO on lobsters (Homarus americanus) from the Canadian maritimes were examin4d for stock differences with the object of defining lobster population bot ndaries. Using pattern recognition techniques, historical lobster landings (1892-1981) from 32 areas resulted in grouping the landing trends into 7-8 areas. Examination of morphometrics data, landing trends, population parameters (growth and size at aturity), movement of tagged lobsters, and general surface currents that might indicate larval drift, suggested the following general lobster stock areas: Western maritimes which included the Bay of Fundy, inshore and possibly offshore) southwestner Nova Scotia (to Shelburne Co.), The Eastern Coast of Nova Scotia (Queens to Cape Breton Counties) which seems to be a transition zone f,r lobsters between the Gulf of Maine and the Gulf of St. Lawrence, and 3. Southern Gulf of St. Lawrence STOCK DISCRI INATION SYMPOSIUM Key words: Homarus americanus; lobsters; stocks; population dynamics; morphonietrics; landing statistics; electrophoresis; recruitment; tagging; movement. General Introduction Historically, there have been various debates amongst biologists, fishery managers, and fishermen as to the geographic discreteness of lobster (Homarus americanus) populations on the Atlantic Coast of North America (eg. -
Luís M.D. Barcelos1, 2*, José M.N. Azevedo1, 3, Jürgen Pollerspöck4, and João P
ACTA ICHTHYOLOGICA ET PISCATORIA (2018) 48 (2): 189–194 DOI: 10.3750/AIEP/02436 REVIEW OF THE RECORDS OF THE SMALLTOOTH SAND TIGER SHARK, ODONTASPIS FEROX (ELASMOBRANCHII: LAMNIFORMES: ODONTASPIDIDAE), IN THE AZORES Luís M.D. Barcelos1, 2*, José M.N. Azevedo1, 3, Jürgen Pollerspöck4, and João P. Barreiros1, 2 1Centre for Ecology, Evolution, and Environmental Changes, Azorean Biodiversity Group, Angra do Heroísmo, Portugal 2Faculty of Agricultural and Environmental Sciences, University of the Azores, Angra do Heroísmo, Portugal 3Faculty of Sciences and Technology, University of the Azores, Ponta Delgada, Portugal 4Bavarian State Collection of Zoology, Munich, Germany Barcelos L.M.D., Azevedo J.M.N., Pollerspöck J., Barreiros J.P. 2018. Review of the records of the smalltooth sand tiger shark, Odontaspis ferox (Elasmobranchii: Lamniformes: Odontaspididae), in the Azores. Acta Ichthyol. Piscat. 48 (2): 189–194. Abstract. In recent years Azorean fishermen reported the presence of the smalltooth sand tiger shark,Odontaspis ferox (Risso, 1810), a very rare demersal shark species, associated with insular shelves and slopes, with occasional incursions into shallow waters and of poorly known biology and ecology. There are fourteen new records of this species, between 1996 and 2014, captured by spearfishing, harpoons, hand lines, or entangled in fishing gear in the Azores. These records were analysed and complemented with fishermen interviews, providing new locations and new biological data for this species. Also, specimens photographs were studied and post-mortem analysis were carefully carried out in one individual. This species is rare and captured only as bycatch in shallow waters. More detailed information on this species is critically needed in order to assess its conservation status and implement management guidelines. -
The Great White Shark Quick Questions
The Great White Shark Quick Questions 11 Great white sharks are the top of the ocean’s food chain. 1. Why do you think that the great white shark is at 22 They are the biggest fish on our planet which eat other the top of the ocean’s food chain? 32 fish and animals. They are known to live between thirty 45 and one hundred years old and can be found in all of the 55 world’s oceans, but they are mostly found in cool water 59 close to the coast. 2. Where are most great white sharks found? 69 Even though they are mostly grey, they get their name 78 from their white underbelly. The great white shark has 89 been known to grow up to six metres long and have 99 up to three hundred sharp teeth, in seven rows. Their 3. Find and copy the adjective that the author uses 109 amazing sense of smell allows them to hunt for prey, to describe the shark’s sense of smell. 119 such as seals, rays and small whales from miles away. 4. Number these facts from 1 to 3 to show the order they appear in the text. They live between thirty and one hundred years. They can grow up to six metres long. They have up to three hundred teeth. The Great White Shark Answers 11 Great white sharks are the top of the ocean’s food chain. 1. Why do you think that the great white shark is at 22 They are the biggest fish on our planet which eat other the top of the ocean’s food chain? 32 fish and animals. -
Order LAMNIFORMES ODONTASPIDIDAE Sand Tiger Sharks Iagnostic Characters: Large Sharks
click for previous page Lamniformes: Odontaspididae 419 Order LAMNIFORMES ODONTASPIDIDAE Sand tiger sharks iagnostic characters: Large sharks. Head with 5 medium-sized gill slits, all in front of pectoral-fin bases, Dtheir upper ends not extending onto dorsal surface of head; eyes small or moderately large, with- out nictitating eyelids; no nasal barbels or nasoral grooves; snout conical or moderately depressed, not blade-like;mouth very long and angular, extending well behind eyes when jaws are not protruded;lower labial furrows present at mouth corners; anterior teeth enlarged, with long, narrow, sharp-edged but unserrated cusps and small basal cusplets (absent in young of at least 1 species), the upper anteriors separated from the laterals by a gap and tiny intermediate teeth; gill arches without rakers; spiracles present but very small. Two moderately large high dorsal fins, the first dorsal fin originating well in advance of the pelvic fins, the second dorsal fin as large as or somewhat smaller than the first dorsal fin;anal fin as large as second dorsal fin or slightly smaller; caudal fin short, asymmetrical, with a strong subterminal notch and a short but well marked ventral lobe. Caudal peduncle not depressed, without keels; a deep upper precaudal pit present but no lower pit. Intestinal valve of ring type, with turns closely packed like a stack of washers. Colour: grey or grey-brown to blackish above, blackish to light grey or white, with round or oval dark spots and blotches vari- ably present on 2 species. high dorsal fins upper precaudal eyes without pit present nictitating eyelids intestinal valve of ring type Habitat, biology, and fisheries: Wide-ranging, tropical to cool-temperate sharks, found inshore and down to moderate depths on the edge of the continental shelves and around some oceanic islands, and in the open ocean. -
Great White Shark) on Appendix I of the Convention of International Trade in Endangered Species of Wild Fauna and Flora (CITES)
Prop. 11.48 Proposal to include Carcharodon carcharias (Great White Shark) on Appendix I of the Convention of International Trade in Endangered Species of Wild Fauna and Flora (CITES) A. PROPOSAL ..............................................................................................3 B. PROPONENT............................................................................................3 C. SUPPORTING STATEMENT....................................................................3 1. Taxonomy.........................................................................................................................3 1.1 Class.................................................................................................................................... 1.2 Order................................................................................................................................... 1.3 Family ................................................................................................................................. 1.4 Species ................................................................................................................................ 1.5 Scientific Synonyms............................................................................................................. 1.6 Common Names .................................................................................................................. 2. Biological Parameters......................................................................................................3 -
The Denticle Surface of Thresher Shark Tails: Three-Dimensional Structure and Comparison to Other Pelagic Species
Received: 3 April 2020 Revised: 14 May 2020 Accepted: 21 May 2020 DOI: 10.1002/jmor.21222 RESEARCH ARTICLE The denticle surface of thresher shark tails: Three-dimensional structure and comparison to other pelagic species Meagan Popp1 | Connor F. White1 | Diego Bernal2 | Dylan K. Wainwright1 | George V. Lauder1 1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Abstract Massachusetts Shark skin denticles (scales) are diverse in morphology both among species and 2 Department of Biology, University of across the body of single individuals, although the function of this diversity is poorly Massachusetts Dartmouth, Dartmouth, Massachusetts understood. The extremely elongate and highly flexible tail of thresher sharks pro- vides an opportunity to characterize gradients in denticle surface characteristics Correspondence George V. Lauder, Museum of Comparative along the length of the tail and assess correlations between denticle morphology and Zoology, 26 Oxford Street, Cambridge, MA tail kinematics. We measured denticle morphology on the caudal fin of three mature 02138. Email: [email protected] and two embryo common thresher sharks (Alopias vulpinus), and we compared thresher tail denticles to those of eleven other shark species. Using surface Funding information National Oceanic and Atmospheric profilometry, we quantified 3D-denticle patterning and texture along the tail of Administration, Grant/Award Number: threshers (27 regions in adults, and 16 regions in embryos). We report that tails of NA16NMF4270231; National Science Foundation, Grant/Award Numbers: IOS- thresher embryos have a membrane that covers the denticles and reduces surface 1354593, GRF DGE-1144152; Office of Naval roughness. In mature thresher tails, surfaces have an average roughness of 5.6 μm Research, Grant/Award Numbers: N00014-09-1-0352, N000141410533 which is smoother than some other pelagic shark species, but similar in roughness to blacktip, porbeagle, and bonnethead shark tails. -
East Bay Hills Wind Project Mi'kmaq Ecological Knowledge Study
East Bay Hills Wind Project Mi’kmaq Ecological Knowledge Study Prepared for: Cape Breton Hydro Inc. December 2012 – Version 1 M.E.K.S. Project Team Jason Googoo, Project Manager Dave Moore, Author and Research Craig Hodder, Author and GIS Technician Mary Ellen Googoo, MEKS Interviewer John Sylliboy, MEKS Traditionalist Prepared by: Reviewed by: ___________________ ____________________ Craig Hodder, Author Jason Googoo, Manager Executive Summary This Mi’kmaq Ecological Knowledge Study, also commonly referred to as an MEKS or a Traditional Ecological Knowledge Study (TEKS), was developed by Membertou Geomatics Solutions (MGS) on behalf of Cape Breton Hydro Inc. (CBHI) for the proposed East Bay Hills Wind Power Project. This MEKS mandate is to consider land and water areas which the proposed project will utilize, and to identify what Mi’kmaq traditional use activities have occurred, or are currently occurring within, and what Mi’kmaq ecological knowledge presently exists in regards to the area. In order to ensure accountability and ethic responsibility of this MEKS, the MEKS development has adhered to the “Mi’kmaq Ecological Knowledge Protocol”. This protocol is a document that has been established by the Assembly of Nova Scotia Mi’kmaq Chiefs, which speaks to the process, procedures and results that are expected of a MEKS. The Mi’kmaq Ecological Knowledge Study consisted of two major components: • Mi’kmaq Traditional Land and Resource Use Activities , both past and present, • A Mi’kmaq Significance Species Analysis , considering the resources that are important to Mi’kmaq use. The Mi’kmaq Traditional Land and Resource Use Activities component utilized interviews as the key source of information regarding Mi’kmaq use in the Project Site and Study Area. -
Population Structure and Biology of Shortfin Mako, Isurus Oxyrinchus, in the South-West Indian Ocean
CSIRO PUBLISHING Marine and Freshwater Research http://dx.doi.org/10.1071/MF13341 Population structure and biology of shortfin mako, Isurus oxyrinchus, in the south-west Indian Ocean J. C. GroeneveldA,E, G. Cliff B, S. F. J. DudleyC, A. J. FoulisA, J. SantosD and S. P. WintnerB AOceanographic Research Institute, PO Box 10712, Marine Parade 4056, Durban, South Africa. BKwaZulu-Natal Sharks Board, Private Bag 2, Umhlanga Rocks 4320, South Africa. CFisheries Management, Department of Agriculture, Forestry and Fisheries, Private Bag X2, Rogge Bay 8012, South Africa. DNorwegian College of Fishery Science, University of Tromsø, NO-9037, Tromsø, Norway. ECorresponding author. Email: [email protected] Abstract. The population structure, reproductive biology, age and growth, and diet of shortfin makos caught by pelagic longliners (2005–10) and bather protection nets (1978–2010) in the south-west Indian Ocean were investigated. The mean fork length (FL) of makos measured by observers on longliners targeting tuna, swordfish and sharks was similar, and decreased from east to west, with the smallest individuals occurring near the Agulhas Bank edge, June to November. Nearly all makos caught by longliners were immature, with equal sex ratio. Makos caught by bather protection nets were significantly larger, males were more frequent, and 93% of males and 55% of females were mature. Age was assessed from band counts of sectioned vertebrae, and a von Bertalanffy growth model fitted to sex-pooled length-at-age data predicted a À1 birth size (L0) of 90 cm, maximum FL (LN) of 285 cm and growth coefficient (k) of 0.113 y . -
Porbeagle Shark Lamna Nasus
Porbeagle Shark Lamna nasus Lateral View (♀) Ventral View (♀) COMMON NAMES APPEARANCE Porbeagle Shark, Atlantic Mackerel Shark, Blue Dog, Bottle-nosed • Heavily built but streamlined mackerel shark. Shark, Beaumaris Shark, Requin-Taupe Commun (Fr), Marrajo • Moderately long conical snout with a relatively large eyes. Sardinero (Es), Tiburón Sardinero (Es), Tintorera (Es). • Large first dorsal fin with a conspicuous white free rear tip. SYNONYMS • Second dorsal fin and anal fin equal-sized and set together. Squalus glaucus (Gunnerus, 1758), Squalus cornubicus (Gmelin, 1789), • Lunate caudal fin with strong keel and small secondary keel. Squalus pennanti (Walbaum, 1792), Lamna pennanti (Desvaux, 1851), Squalus monensis (Shaw, 1804), Squalus cornubiensis (Pennant, 1812), • Dorsally dark blue to grey with no patterning. Squalus selanonus (Walker, 1818), Selanonius walkeri (Fleming, 1828), • Ventrally white. Lamna punctata (Storer, 1839), Oxyrhina daekyi (Gill, 1862), Lamna • Maximum length of 365cm, though rarely to this size. NE MED ATL philippi (Perez Canto, 1886), Lamna whitleyi (Phillipps, 1935). DISTRIBUTION The Porbeagle Shark is a large, streamlined mackerel shark with a In the northern conical snout and powerful body. The first dorsal fin is large and hemisphere, the originates above or slightly behind the pectoral fins. It has a free rear Porbeagle Shark tip which is white. The second dorsal fin is tiny and is set above the occurs only in the anal fin, to which it is comparable in size. The caudal fin is strong and North Atlantic and lunate with a small terminal notch. The caudal keel is strong and, Mediterranean, uniquely for the northeast Atlantic, a smaller secondary caudal keel is whilst in the present. -
8Th MEETING of the SCIENTIFIC COMMITTEE New Zealand, 3 to 8 October 2020
th 8 MEETING OF THE SCIENTIFIC COMMITTEE New Zealand, 3 to 8 October 2020 SC8-DW14 Interactions with marine mammals, seabirds, reptiles, other species of concern New Zealand PO Box 3797, Wellington 6140, New Zealand P: +64 4 499 9889 – F: +64 4 473 9579 – E: [email protected] www.sprfmo.int SC8-DW14 South Pacific Regional Fisheries Management Organisation 8th Meeting of the Scientific Committee Online meeting hosted by New Zealand, 3–8 October 2020 Interactions with marine mammals, seabirds, reptiles (turtles), and other species of concern in bottom fisheries to 2019 Martin Cryer1, Igor Debski2, Shane W. Geange2, Tiffany D. Bock3, Marco Milardi3 3 September 2020 1. Fisheries New Zealand, Ministry for Primary Industries, Nelson, New Zealand 2. Department of Conservation, Wellington, New Zealand 3. Fisheries New Zealand, Ministry for Primary Industries, Wellington, New Zealand 1 SC8-DW14 Contents 1. Purpose of paper ............................................................................................................. 3 2. Requirements of CMM-03-2020 and CMM-02-2020 ....................................................... 3 3. Reported interactions ..................................................................................................... 3 4. Discussion of seabird interactions ................................................................................... 5 5. Processes for verifying records and updating databases ................................................. 6 6. Acknowledgments .......................................................................................................... -
MD Shark Catch Card
Live Releases Dead Releases TODAY’S DATE: DATE: TODAY’S MM Write the # of sharks released alive in the Live Releases Box and the # released dead Maryland Shark in the Dead Release Box. DD Catch Card YYYY Today’s Date: MM DD YYYY Species (see reverse for list): If you cannot ID, you MUST release it Shark TAG #: Shark TAG HMS PERMIT #: Was this fish caught during a tournament? Yes / No Tournament Name: Fork Length Tagging Location Reporting Station: *Measurement Description Shark Tag #: * Measure in a straight line from the tip of the (Obtain at Reporting Station) Sex (circle one): M / F snout to the fork of the tail. *Fork Length (inches): **Weight (lbs) ** Scale weight ONLY. Do not record estimated weight. Complete this section if fishing from a vessel: NOTE: Most sharks landed in Maryland must have Vessel Name: a LANDING TAG affixed before removal from the vessel. Tags are available at all SHARK REPORTING STATIONS. To obtain a LANDING TAG, captains or Registration # (State ID): operators of the permitted vessel, or licensed angler if fishing from shore, must complete and submit a Permit Holders Name: catch card for every shark landed. For a complete Atlantic HMS list of sharks that you must report, please see the Permit #: reverse side of this card. Trip Type: Charter / Private / Headboat This information collected is approved under OMB (Circle One) Control # 0648-0328 and expires on 07/31/2019 Live Releases Dead Releases TODAY’S DATE: DATE: TODAY’S MM Write the # of sharks released alive in the Live Releases Box and the # released dead Maryland Shark in the Dead Release Box.